| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001193270.2 | 684 | Missense Mutation | CAC,CAG | H191Q | NP_001180199.1 |
| NM_001282174.1 | 684 | Missense Mutation | CAC,CAG | H54Q | NP_001269103.1 |
| NM_006800.3 | 684 | Missense Mutation | CAC,CAG | H37Q | NP_006791.2 |
| NM_078628.1 | 684 | Intron | NP_523352.1 | ||
| NM_078629.3 | 684 | Missense Mutation | CAC,CAG | H203Q | NP_523353.2 |